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In this model, the neuroprotective capacity of Cr in the hypoxic perinatal brain is attributed to reduced lipid peroxidation and apoptosis, likely through maintained mitochondrial function [71].
Wang et al. (2008) have shown that RIC in vivo using limb preconditioning generated a dialysate, which protected naïve perfused rabbit hearts against the myocardial IRI in terms of preserved outer mitochondrial membrane (OMM) integrity and maintained mitochondrial function.
In addition, inorganic phosphate increased caspase-3 activity and decreased the mitochondrial membrane potential, whereas NOS inhibitors maintained mitochondrial function, illustrating that NO mediates phosphate-dependent chondrocyte apoptosis [ 29].
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Taken together, these data identify Clu as a mitochondrially-associated protein that plays a direct role in maintaining mitochondrial function and that binds TOM20, and support a role for Clu linking mitochondrial function to the PINK1-Park pathway.
We also demonstrate that Blm10 acts to maintain mitochondrial function.
Chen, Y.-C. Y.-C.. Msp1/ATAD1 maintains mitochondrial function by facilitating thetdegralation of Msp1/ATAD1ed tail-anchored proteins.
These processes serve to maintain mitochondrial function and ensure optimal energy supply for the cell.
These data demonstrate that tumour elicited c-Kit signalling drives both the increase in neutrophil number and mitochondrial fitness resulting in an oxidative population of neutrophils which use fatty acid metabolism to maintain mitochondrial function.
Conclusion: The results indicate that preterm fetuses are more capable than term fetuses of maintaining mitochondrial function under conditions of transient intrauterine ischemia and suggest that oxygenderived free radicals may play a crucial role in the development of neonatal neurologic deficit.
We examined the critical roles played by the antioxidant, non-protein thiol, glutathione and related enzyme, glutaredoxin in maintaining mitochondrial function during excitotoxicity caused by β-N-oxalyl amino-l-alanine (l-BOAA), the causative factor of neurolathyrism, a motor neuron disease involving the pyramidal system.
In other terms, the failure of maintaining mitochondrial function through biogenesis may contribute to bad outcome.
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